Corpus 1,276 assessed · 1,177 scored · 644 reproduced ≥75 · 170 flagged ·∅ 74/100

Publications 4 Datasets 392.5k Experiments 4.7k

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4 matching publication(s)

Publication	Journal	Year	Score	Verdict
A Deeper Insight into Evolutionary Patterns and Phylogenetic History of ASFV Epidemics in Sardinia (Italy) through Extensive Genomic Sequencing. PMID 34696424	Viruses	2021	76	L1 76/100
Exome sequencing in 38 patients with intracranial aneurysms and subarachnoid hemorrhage. ⚑ PMID 32367296	—	2020	78	78/100 ⚑
Evaluating sequence data quality from the Swift Accel-Amplicon CFTR Panel. PMID 31913291	Sci Data	2020	89	L1 89/100
An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome. PMID 24781758	—	2015	83	L1 83/100

A Deeper Insight into Evolutionary Patterns and Phylogenetic History of ASFV Epidemics in Sardinia (Italy) through Extensive Genomic Sequencing.

PMID 34696424 · Viruses · 2021

L1 76/100

Exome sequencing in 38 patients with intracranial aneurysms and subarachnoid hemorrhage.⚑

PMID 32367296 · · 2020

78/100 ⚑

Evaluating sequence data quality from the Swift Accel-Amplicon CFTR Panel.

PMID 31913291 · Sci Data · 2020

L1 89/100

An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome.

PMID 24781758 · · 2015

L1 83/100